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Randomised clinical study: acute effects of metformin versus placebo on portal pressure in patients with cirrhosis and portal hypertension

医学 二甲双胍 内科学 安慰剂 吲哚青绿 胃肠病学 肝硬化 门脉高压 门静脉压 血压 外科 病理 替代医学 胰岛素
作者
Nikolaj Rittig,Niels Kristian Aagaard,Gerda Elisabeth Villadsen,Thomas Damgaard Sandahl,Niels Jessen,Henning Grønbæk,Jacob George
出处
期刊:Alimentary Pharmacology & Therapeutics [Wiley]
卷期号:54 (3): 320-328 被引量:14
标识
DOI:10.1111/apt.16460
摘要

Summary Background Portal hypertension is the main determinant of clinical decompensation in patients with liver cirrhosis. In preclinical data metformin lowers portal pressure, but there are no clinical data for this beneficial effect. Aims To investigate the acute effects of metformin on hepatic venous pressure gradient (HVPG) and liver perfusion. Methods In a randomised, double‐blinded study design, we investigated 32 patients with cirrhosis before and 90 minutes after ingestion of 1000‐mg metformin (n = 16) or placebo (n = 16). Liver vein catherisation was performed to evaluate HVPG and indocyanine green (ICG) infusion for investigation of hepatic blood flow. Results The mean relative change in HVPG was −16% (95% CI: −28% to −4%) in the metformin group compared with 4% (95% CI: −6% to 14%) in the placebo group (time × group interaction, P = 0.008). In patients with baseline HVPG ≥12 mm Hg clinically significant improvements in HVPG (HVPG <12 mm Hg or a >20% reduction in HVPG) were observed in 46% (6/13) of metformin‐treated and in 8% (1/13) of placebo‐treated patients ( P = 0.07). There were no changes or differences in systemic blood pressure, heart rate, hepatic plasma and blood flow, hepatic ICG clearance, hepatic O 2 uptake or inflammation markers between groups. Conclusions A single oral metformin dose acutely reduces HVPG in patients with portal hypertension without affecting systemic or liver hemodynamics or inflammatory biomarkers. This offers a promising perspective of a safe and inexpensive treatment option that should be investigated in larger‐scale clinical studies with long‐term outcomes in patients with cirrhosis and portal hypertension.
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